Baek Grace T, Mathis Noah J, Perissinotti Anthony J, Marini Bernard L, Brown Anna, Phillips Tycel J, Wilcox Ryan A, Nachar Victoria R
Department of Pharmacy Services and Clinical Pharmacy, Michigan Medicine, Ann Arbor, MI, USA.
Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, MI, USA.
Leuk Lymphoma. 2021 Dec;62(13):3138-3146. doi: 10.1080/10428194.2021.1953014. Epub 2021 Jul 15.
Bendamustine is a preferred first-line chemoimmunotherapy regimen for indolent non-Hodgkin's lymphoma (iNHL). Emerging evidence suggests an increased incidence of late-onset complications with bendamustine-based regimens compared with CHOP/CVP; however, this evidence is limited. We retrospectively compared late-onset complications from January 2005 to May 2020 in adults with previously untreated iNHL who received rituximab or obinutuzumab with CHOP, CVP, or bendamustine. Forty-six patients received CHOP/CVP; 119 received bendamustine. No difference in incidence of late-onset infections was observed. Bendamustine led to a higher rate of prolonged and unresolved lymphocytopenia and a greater incidence of late-onset neutropenia. Many patients receiving bendamustine did not have lymphocyte recovery even three years following administration. Ongoing infection prophylaxis with bendamustine-based regimens may offset translation of these laboratory findings to late-onset infectious risk.
苯达莫司汀是惰性非霍奇金淋巴瘤(iNHL)首选的一线化疗免疫治疗方案。新出现的证据表明,与CHOP/CVP相比,基于苯达莫司汀的方案导致迟发性并发症的发生率增加;然而,这方面的证据有限。我们回顾性比较了2005年1月至2020年5月期间接受利妥昔单抗或奥妥珠单抗联合CHOP、CVP或苯达莫司汀治疗的既往未治疗的成人iNHL患者的迟发性并发症。46例患者接受CHOP/CVP治疗;119例接受苯达莫司汀治疗。未观察到迟发性感染发生率的差异。苯达莫司汀导致淋巴细胞减少持续时间延长和未缓解的发生率更高,迟发性中性粒细胞减少的发生率更高。许多接受苯达莫司汀治疗的患者即使在给药三年后淋巴细胞也未恢复。基于苯达莫司汀的方案持续进行感染预防可能会抵消这些实验室检查结果转化为迟发性感染风险。